Controlled release of DNA from self-degrading microcapsules

Self -disintegrating microcapsules were prepared by encapsulating a highly active mix of proteases (Pronase (R)) into biodegradable polyelectrolyte shells. Pronase was captured by micron-sized calcium carbonate particles that were subsequently embedded into onion-like shells Of pOly(L-arginine) and Poly(L-aspartic acid). EDTA treatment was used to extract the calcium carbonate constituents from the resulting core-shell particles. As a consequence, Pronase was released into the capsule interior and started to digest the surrounding polyelectrolyte shell. Lifetimes of such self-disintegrating capsules could be successfully adjusted to seconds, hours or days by varying the amount of encapsulated Pronase. The enzyme -mediated, sustained release of encapsulated DNA is presented as a prospective